Team:Biwako Nagahama/Project
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== <h2>Agrepaper</h2> == | == <h2>Agrepaper</h2> == | ||
=== <h2>Background</h2> === | === <h2>Background</h2> === | ||
- | <p>There are variety of problems all over the world today.For example, there are global warming, destruction of the ozone layer, | + | <p>There are variety of problems all over the world today.For example, there are global warming, destruction of the ozone layer, mass extinction, energy problem, desertification and lack of water.There problems are caused by deforestation.</p> |
<p>②How to solve it.</p> | <p>②How to solve it.</p> | ||
<p>③Environment issues can solve if not to use wood as well as burdon the environment. | <p>③Environment issues can solve if not to use wood as well as burdon the environment. |
Revision as of 18:39, 27 September 2013
Contents |
AgRePaper&E.coli-ink
Cellulose is used as raw material for paper, so our team experimented various ways to increase the amount of cellulose produced by agrobacterium and using it to make papers. For this we developed the different parts to insert into the system of agrobacterium. Among them are the genes used for expression of the curdlan. Similarly, genetic parts in order to increase the expression of the cellulose, along with the agrobacterium type binary vector were also developed . We are also working on recycling the produced paper by degrading the cellulose to D-Glucose using various enzymes. We worked for the preparation of the biological ink using the sperm whale's cells by genetically modification to increase amount of myoglobin. Then, we observed the change on the color of the product by altering the formation of myoglobin and the production amount of myoglobin with the insertion of T7 promoter to the cell system.
Agrepaper
Background
There are variety of problems all over the world today.For example, there are global warming, destruction of the ozone layer, mass extinction, energy problem, desertification and lack of water.There problems are caused by deforestation.
②How to solve it.
③Environment issues can solve if not to use wood as well as burdon the environment. We need to know “What is the paper?” to think the method.
④The main component of paper is cellulose and hemicellulose.
⑤We were confirmed by Nakasima’s experiments that Agrobacterium make cellulose. Agrobacterium can’t make hemicellulose but cardlan Agrobacterium made has potential instead of hemicellulose, Ootaki perform confimatory experiment .As a result cardlan is able to instead of hemicellulose.
Secretion of fibrils from Agro
For this year’s project our team aimed at making the paper by using Agro bacterium. So, we confirmed whether carbohydrate developed from Agrobacterium could be used as the raw material for making paper.
Materials
Agro bacterium tumefaciens C58
Agro bacterium tumefaciens C58 bacterial liquid
+LB medium 2 ml
+ampicillin 2 µl
+Agro bacterium tumefaciens C58
Congo red
LB medium
+1.0%(w/v) Triptone 2 g
+0.5%(w/v) yeast extract 1 g
+1.0%(w/v) NaCl 2 g
Experiment1
Sample 1 curdlan 15 µl +Congo red 5 µl +Agro bacterium precipitation
Sample 2 de-ionized water 15 µl +Congo red 5 µl +Agro bacterium precipitation
We centrifuged Sample 1 and 2 in 5 minutes with cooled centrifuges(4 ℃,13000 rpm).
As a result, Sample 1 had red precipitates. Sample 2 rationally melted.
So, we confirmed the presence of carbohydrate in the precipitates obtained from Agro bacterium.
Experiment2
Next, we found that carbohydrate could be produced when soy milk is added to the fluid bacteria
So, we experimented for the confirmation of the above findings.
Sample 3 LB medium 7 ml +Agro bacterium+soy 40 µl
Sample 4 LB medium 7 ml +Agro bacterium
Sample 5 LB medium 7 ml +soy 40 µl
Sample 6 LB medium 7 ml
We cultivated Sample 3 ~ 6 at 28 ℃.for 12 hours
Then, Sample1 and 2 produced a white film like substance but Sample 3 and 4 did not.
We put the white films from Sample 1 and 2 into micro-tubes.
Sample3 Sample4
Sample 7 supernatant(Sample 1) 15 µl +Congo red 5 µl
Sample 8 supernatant(Sample 1) 15 µl +Congo red 5 µl +de-ionized water 1 ml
Sample 9 supernatant(Sample 2) 15 µl +Congo red 5 µl
Sample 10 supernatant(Sample 2) 15 µl +Congo red 5 µl +de-ionized water 1 ml
Sample 11 Congo red 5 µl +de-ionized water 1 ml
We centrifuged all the samples for 5 minutes at 4 ℃,13000 rpm.
As a result, Sample 7 ~ 10 gave red precipitates but Sample 11 did not.
So, we confirmed Sample 7 ~ 10 had carbohydrate.
Through these experiments, we confirmed that Agro bacterium can discharge carbohydrate without soy milk.
Reference
1, Laboratory maintenance of Agrobacterium.
(http://europepmc.org/articles/PMC3350319)
2, Coordination of Division and Development Influences Complex Multicellular Behavior in Agrobacterium tumefaciens (Jinwoo Kim.¤, Jason E. Heindl., Clay Fuqua)
3, Kirin Kyowa Foods Company (http://www.kirinkyowa-foods.co.jp/products/curdlan/)
4, Howard Hughes Molecular Biology Summer Research Program Poster, Austin, TX , August, 1995 Microcopy of Curdlan Structure
5, Iain M. Cheeseman and R.Malcom Brown,Jr, Department of Botanty , The University of Texas at Austin,TX,78713
(http://www.botanty.utexas.edu/facstaff/facpages/mbroun/ongres/icheeze.htm)
About curdlan
Agrobacterim makes carbohydrate chain. For exampe it makes curdlan on culture midium.We'll explain curdlan on this page.
About curdlan
It is fermentative polysaccharide that microorganizm makes. It polymerizes two position;C₁and C₃on D-glucose. Its binding position is not straight. So it is cycloid structure.
File:Biwako-nagahama curdlan's-picture yoshiharu-otaki1.png
CrdS
Cloning of CrdS and Restriction Enzyme
By Koki Tsutsumi
CrdS gene had produced clone from Agrobacterium tumefaciens C58, but I confirmed whether it’s true or not. CrdS gene has restriction enzyme sites,EcoRI and PstI.